{{Rsnum
|rsid=1165472
|Chromosome=1
|position=55642931
|Orientation=plus
|GMAF=0.2153
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 8.0 | 32.7 | 59.3
| HCB | 0.7 | 19.7 | 79.6
| JPT | 0.0 | 13.3 | 86.7
| YRI | 10.3 | 45.2 | 44.5
| ASW | 8.8 | 24.6 | 66.7
| CHB | 0.7 | 19.7 | 79.6
| CHD | 0.9 | 19.3 | 79.8
| GIH | 5.9 | 45.5 | 48.5
| LWK | 14.5 | 47.3 | 38.2
| MEX | 1.7 | 19.0 | 79.3
| MKK | 10.3 | 38.5 | 51.3
| TSI | 6.9 | 35.3 | 57.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23776197
  |Trait=Paclitaxel-induced neuropathy
  |Title=Genome-wide association study identifies ephrin type A receptors implicated in paclitaxel induced peripheral sensory neuropathy.
  |RiskAllele=G
  |Pval=4E-6
  |OR=2.36
  |ORtxt=[1.64-3.40]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}